Visitor Monitoring Drug History: DIAMOX
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: DIAMOX
FDA Application No: (NDA) 012945
Active Ingredient(s): ACETAZOLAMIDE
Company: DURAMED PHARMS BARR
 
Label History
 
View the label approved on March 18, 2005 for DIAMOX, (NDA) 012945


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/15/2005 038Labeling Revision Letter
Label 
3/15/2005 037Manufacturing Change or Addition Letter
Label 
9/27/1999 030Control Supplement  
4/25/1995 028Formulation Revision  
 
There are no Therapeutic Equivalents
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